Corticobasal degeneration

March 2000
Journal of Neurology, Neurosurgery & Psychiatry;Mar2000, p275
Academic Journal
No abstract available.


Related Articles

  • Dysarthria and Pathological Laughter/Crying as Presenting Symptoms of Corticobasal- Ganglionic Degeneration Syndrome. Thümler, B. H.; Urban, P. P.; Davids, E.; Siessmeier, M.; Schreckenberger, T.; Benz, P.; Stoeter, P.; Bartenstein, P.; Hopf, H. C. // Journal of Neurology;Sep2003, Vol. 250 Issue 9, p1107 

    Presents a letter to the editor concerning symptoms of corticobasal-ganglionic degeneration syndrome.

  • corticobasal degeneration.  // Taber's Cyclopedic Medical Dictionary (2009);2009, Issue 21, p532 

    An encyclopedia entry for "corticobasal degeneration," which refers to a neurological disease wherein the brain cells die in the basal ganglia and the brain cortex, is presented.

  • Amantadine/domperidone.  // Reactions Weekly;Jul2015, Vol. 1559 Issue 1, p23 

    An abstract of the article "Neuroleptic Malignant Syndrome in an Elderly Patient With Normal Pressure Hydrocephalus Overlapping Corticobasal Degeneration," by A. T. Isik and colleagues is presented.

  • From The Archives. Compston, Alastair // Brain: A Journal of Neurology;Jul2010, Vol. 133 Issue 7, p1860 

    The article discusses two reports on corticobasal degeneration that were published in previous issues of "Brain." In the first report, researchers described the cases of several patients with the condition. It is asserted that corticobasal degeneration usually presents with a focal movement...

  • Corticobasal syndrome: a field of uncertainty. Strupp, Michael // Journal of Neurology;Jan2011, Vol. 258 Issue 1, p173 

    The article reviews three articles on corticobasal syndrome "Does corticobasal degeneration exist? A clinicopathological re-evaluation," by H. Ling, which appeared in the periodical "Brain," "Imaging correlates of pathology in corticobasal syndrome," by J.L. Whitwell, which appeared in the...

  • Does corticobasal degeneration exist? A clinicopathological re-evaluation. Ling, Helen; O'Sullivan, Sean S.; Holton, Janice L.; Revesz, Tamas; Massey, Luke A.; Williams, David R.; Paviour, Dominic C.; Lees, Andrew J. // Brain: A Journal of Neurology;Jul2010, Vol. 133 Issue 7, p2045 

    The pathological findings of corticobasal degeneration are associated with several distinct clinical syndromes, and the corticobasal syndrome has been linked with a number of diverse pathologies. We have reviewed all the archival cases in the Queen Square Brain Bank for Neurological Disorders...

  • Kortikobazine degeneracija: literaturos ap�valga ir triju klinikiniu atveju pristatymas. Taraseviciute, E.; �e�eikaite, M.; Sakalauskaite-Juodeikiene, E.; Kaubrys, G.; Budrys, V. // Neurologijos Seminarai;2012, Vol. 16 Issue 2, p109 

    Corticobasal degeneration is a rare disease of un known etiology. It was described by Rebeiz and colleagues as "corticodentatonigral degeneration with neuronal achromasia". Clinically corticobasal degeneration manifests as parkinsonian syndrome with unilateral or asymmetric signs of...

  • Neuropathological features of corticobasal degeneration presenting as corticobasal syndrome or Richardson syndrome. Kouri, Naomi; Murray, Melissa E.; Hassan, Anhar; Rademakers, Rosa; Uitti, Ryan J.; Boeve, Bradley F.; Graff-Radford, Neill R.; Wszolek, Zbigniew K.; Litvan, Irene; Josephs, Keith A.; Dickson, Dennis W. // Brain: A Journal of Neurology;Nov2011, Vol. 134 Issue 11, p3264 

    Patients with corticobasal degeneration can present with several different clinical syndromes, making ante-mortem diagnosis a challenge. Corticobasal syndrome is the clinical phenotype originally described for corticobasal degeneration, characterized by asymmetric rigidity and apraxia, cortical...

  • Diffusion-weighted brain imaging study of patients with clinical diagnosis of corticobasal degeneration, progressive supranuclear palsy and Parkinson's disease. Lodi, Raffaele // Brain: A Journal of Neurology;Dec2009, Vol. 132 Issue 12, pe130 

    A letter to the editor is presented in response to the article "Diffusion-Weighted Brain Imaging Study of Patients With Clinical Diagnosis of Corticobasal Degeneration, Progressive Supranuclear Palsy and Parkinson's Disease" that was published in a previous issue.

  • Familial autosomal dominant cortico-basal degeneration with the P301S mutation in the tau gene: an example of phenotype variability. Casseron, W.; Azulay, J. P.; Guedj, E.; Gastaut, J. L.; Pouget, J. // Journal of Neurology;Dec2005, Vol. 252 Issue 12, p1546 

    The article presents a letter to the editor about "Familial Autosomal Dominant Cortico-Basal Degeneration With the P301S Mutation in Tau Gene: An Example of Phenotype Variability."


Read the Article


Sign out of this library

Other Topics